PMID- 36588396 OWN - NLM STAT- MEDLINE DCOM- 20230216 LR - 20230303 IS - 1096-8652 (Electronic) IS - 0361-8609 (Linking) VI - 98 IP - 3 DP - 2023 Mar TI - Thrombosis in multiple myeloma: Risk estimation by induction regimen and association with overall survival. PG - 413-420 LID - 10.1002/ajh.26806 [doi] AB - Lenalidomide-containing (R) triplet and quadruplet regimens are the standard of care for multiple myeloma (MM) and have been shown to increase the risk of thrombosis. The association between thromboembolism (TE) and survival in the novel multidrug era is not yet delineated. In this study, we evaluated the incidence of TE during the first year of MM diagnosis, its association with the type of induction regimen, and its impact on overall survival. We studied 672 newly diagnosed MM (NDMM) patients who received a triplet or quadruplet lenalidomide-based induction at the Mayo Clinic, Rochester. TE was diagnosed in 83 patients (12.4%). Of these, 56 (8.3%) had a deep venous thrombosis (DVT), 23 (3.4%) had a pulmonary embolism (PE) with or without the DVT, and 4 (0.6%) patients had a stroke. Carfilzomib-Rd (KRd) had the highest risk of TE (21.1%, 18/85), followed by quadruplets (11.1%, 5/45), bortezomib-Rd (9.6%, 51/531), and 0/11 (0%), treated with other lenalidomide-containing regimens. The difference in TE risk between KRd and the other regimens was statistically significant (OR = 2.6, p < .01). Nine patients developed a TE before being exposed to any treatment. Survival was significantly lower among patients that developed a TE (66 vs. 133 months, p < .01). The association of TE with reduced survival demonstrated in univariate analysis (HR = 2.2, 95% CI = 1.6-3.3) was maintained in the multivariable analysis adjusted for high-risk interphase fluorescence in situ hybridization (FISH), sex, age, receipt of an upfront transplant, the response at induction, and the International Staging System (ISS) (HR = 2.61, CI = 1.74-3.9). We conclude that TE is an important aspect of MM management, and effective management is especially relevant in the novel treatment era. CI - (c) 2023 Wiley Periodicals LLC. FAU - Charalampous, Charalampos AU - Charalampous C AUID- ORCID: 0000-0003-3617-3141 AD - Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA. FAU - Goel, Utkarsh AU - Goel U AUID- ORCID: 0000-0003-1663-0325 AD - Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA. FAU - Kapoor, Prashant AU - Kapoor P AD - Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA. FAU - Binder, Moritz AU - Binder M AUID- ORCID: 0000-0001-9014-9658 AD - Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA. FAU - Buadi, Francis K AU - Buadi FK AD - Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA. FAU - Dingli, David AU - Dingli D AD - Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA. FAU - Dispenzieri, Angela AU - Dispenzieri A AUID- ORCID: 0000-0001-8780-9512 AD - Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA. FAU - Fonder, Amie L AU - Fonder AL AD - Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA. FAU - Gertz, Morie A AU - Gertz MA AUID- ORCID: 0000-0002-3853-5196 AD - Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA. FAU - Gonsalves, Wilson AU - Gonsalves W AUID- ORCID: 0000-0001-6890-969X AD - Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA. FAU - Hayman, Suzanne R AU - Hayman SR AD - Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA. FAU - Hobbs, Miriam A AU - Hobbs MA AD - Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA. FAU - Hwa, Yi L AU - Hwa YL AUID- ORCID: 0000-0002-8163-2979 AD - Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA. FAU - Kourelis, Taxiarchis AU - Kourelis T AUID- ORCID: 0000-0001-8573-9434 AD - Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA. FAU - Lacy, Martha Q AU - Lacy MQ AD - Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA. FAU - Leung, Nelson AU - Leung N AUID- ORCID: 0000-0002-5651-1411 AD - Division of Nephrology and Hypertension, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA. FAU - Lin, Yi AU - Lin Y AD - Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA. FAU - Warsame, Rahma AU - Warsame R AUID- ORCID: 0000-0003-0240-0326 AD - Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA. FAU - Kyle, Robert A AU - Kyle RA AD - Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA. FAU - Rajkumar, S Vincent AU - Rajkumar SV AUID- ORCID: 0000-0002-5862-1833 AD - Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA. FAU - Kumar, Shaji AU - Kumar S AUID- ORCID: 0000-0001-5392-9284 AD - Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20230101 PL - United States TA - Am J Hematol JT - American journal of hematology JID - 7610369 RN - F0P408N6V4 (Lenalidomide) RN - 7S5I7G3JQL (Dexamethasone) RN - 69G8BD63PP (Bortezomib) SB - IM MH - Humans MH - *Multiple Myeloma/complications/drug therapy MH - Lenalidomide/therapeutic use MH - In Situ Hybridization, Fluorescence MH - Dexamethasone/therapeutic use MH - Antineoplastic Combined Chemotherapy Protocols/adverse effects MH - Bortezomib/therapeutic use MH - *Thrombosis/etiology/drug therapy MH - *Thromboembolism/drug therapy EDAT- 2023/01/03 06:00 MHDA- 2023/02/17 06:00 CRDT- 2023/01/02 02:03 PHST- 2022/10/27 00:00 [revised] PHST- 2022/09/01 00:00 [received] PHST- 2022/11/28 00:00 [accepted] PHST- 2023/01/03 06:00 [pubmed] PHST- 2023/02/17 06:00 [medline] PHST- 2023/01/02 02:03 [entrez] AID - 10.1002/ajh.26806 [doi] PST - ppublish SO - Am J Hematol. 2023 Mar;98(3):413-420. doi: 10.1002/ajh.26806. Epub 2023 Jan 1.